3-O-p-trans-Coumaroylalphitolic acid

10-hydroxy-9-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid

AQHKWALTXQHZKK-XNTDXEJSSA-N CHEBI:168388 0 Reactome links 2 studies

Metabolite details

Identifier: AQHKWALTXQHZKK-XNTDXEJSSA-N
InChI Key: AQHKWALTXQHZKK-XNTDXEJSSA-N
IUPAC name: 10-hydroxy-9-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid
Preferred name: 3-O-p-trans-Coumaroylalphitolic acid
INN name: —
Synonym: —
ChEBI: CHEBI:168388

Reactome pathways

No Reactome pathways listed for this metabolite.

Observed in studies

Metabolomic Insights into the Browning of the Peel of Bagging ‘Rui Xue’ Apple Fruit
Transcriptomic dynamics control rapid transition of core crop functions in 'lactating' pigeon

Observed in differential profiles

Non_Bagged_Fruits_vs_Bagged_Fruits_With_Browning
Male_19_days_vs_Male_1_day